Full TGIF Record # 35208
Item 1 of 1
Publication Type:
i
Refereed
Author(s):Thelen, Kurt D.; Jackson, Evelyn P.; Penner, Donald
Author Affiliation:Program Manager, Michigan Department of Agriculture, Lansing MI; Specialist, Department of Chemistry, Max T. Rogers NMR Facility; Professor, Department of Crop and Soil Science, Michigan State University, East Lansing, MI.
Title:Characterizing the sethoxydim-bentazon interaction with proton nuclear magnetic resonance spectrometry
Source:Weed Science. Vol. 43, No. 3, July-September 1995, p. 337-341.
Publishing Information:Champaign, IL: Weed Science Society of America
# of Pages:5
Keywords:TIC Keywords: Herbicide interaction; Absorption; Sethoxydim; Bentazon; Antagonism
Abstract/Contents:"The antagonistic effect of Na-bentazon on sethoxydim absorption and herbicidal activity has been documented. The addition of ammonium sulfate (AMS) with a surfactant overcomes the observed loss of sethoxydim activity. Nuclear Magnetic Resonance(NMR) was used to study the chemical effects of commercially formulated Na-bentazon, NaCl, NaHCO³, Na-bentazon plus AMS, and NaHCO³ plus AMS on commercially formulated sethoxydim. Technical grade Lisethoxydim and sethoxydim were analyzed and ₁H-NMR spectra were used as comparative standards. Data indicate an association of Na₊ from Na-bentazon, NaHCO³ and NaCl with the sethoxydim molecule. NH⁴₊ from AMS appears to associate spatially with sethoxydim but does not exert the same electronic effect on the sethoxydim ring protons as observed with Na₊ or Li₊. The addition of AMS to sethoxydim plus Na-bentazon or NaHCO³ treatments prevents the complexation of Na₊ with the sethoxydim molecule. The data support the hypothesis that the observed Na-bentazon antagonism and ammonium sulfate reversal of antagonism are chemically based."
Language:English
References:12
Note:Figures
ASA/CSSA/SSSA Citation (Crop Science-Like - may be incomplete):
Thelen, K. D., E. P. Jackson, and D. Penner. 1995. Characterizing the sethoxydim-bentazon interaction with proton nuclear magnetic resonance spectrometry. Weed Sci. 43(3):p. 337-341.
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